Preimplantation genetic diagnosis for Duchenne muscular dystrophy by multiple displacement amplification Zi Ren, M.D., Ph.D., Hai-tao Zeng, M.D., Ph.D.,

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Preimplantation genetic diagnosis for Duchenne muscular dystrophy by multiple displacement amplification Zi Ren, M.D., Ph.D., Hai-tao Zeng, M.D., Ph.D., Yan-wen Xu, M.D., Ph.D., Guang-lun Zhuang, M.D., Jie Deng, M.D., Ph.D., Cheng Zhang, M.D., Ph.D., Can-quan Zhou, M.D. Fertility and Sterility Volume 91, Issue 2, Pages 359-364 (February 2009) DOI: 10.1016/j.fertnstert.2007.11.044 Copyright © 2009 American Society for Reproductive Medicine Terms and Conditions

Figure 1 Case 1: PGD for a female carrier with a duplication of exons 3–11 in the dystrophin gene. Arrows indicate where familial mutations are located. Npat and Nmat correspond to paternal and maternal normal dystrophin haplotype, respectively. Dup represents dystrophin duplication haplotype. Fertility and Sterility 2009 91, 359-364DOI: (10.1016/j.fertnstert.2007.11.044) Copyright © 2009 American Society for Reproductive Medicine Terms and Conditions

Figure 2 Case 2: PGD for a female carrier with a deletion of exons 47–50. Arrows indicate where familial mutations are located. Npat and Nmat correspond to paternal and maternal normal dystrophin haplotype, respectively. Del represents dystrophin deletion haplotype. Fertility and Sterility 2009 91, 359-364DOI: (10.1016/j.fertnstert.2007.11.044) Copyright © 2009 American Society for Reproductive Medicine Terms and Conditions